Bai N - Search Results

1

[Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree].

Kang H, Bai N, Mei S, Kong X. Kang H, et al. Among authors: bai n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):184-187. doi: 10.3760/cma.j.issn.1003-9406.2018.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652988 Chinese.

2

[Genetic analysis of a patient featuring developmental delay and mental retardation].

Bai N, Liu Y, Mei S, Kong X. Bai N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):208-11. doi: 10.3760/cma.j.issn.1003-9406.2016.02.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27060317 Chinese.

3

[SNP array and cytogenetic analysis of a patient with unexplained mental retardation].

Bai N, Mei S, Zhao Z, Kong X. Bai N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):332-4. doi: 10.3760/cma.j.issn.1003-9406.2016.03.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264815 Chinese.

4

[Genetic analysis of a rare case with Kallman syndrome and steroid sulfatase deficiency].

Liu X, Bai N, Kong X. Liu X, et al. Among authors: bai n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):349-52. doi: 10.3760/cma.j.issn.1003-9406.2016.03.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264819 Chinese.

5

[Detection and genetic counseling of F8 gene inversions for patients with severe hemophilia A].

Bai N, Wu Q, Liu N, Chen D, Zhao Z, Kong X. Bai N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):508-10. doi: 10.3760/cma.j.issn.1003-9406.2016.04.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27455009 Chinese.

6

[Genetic analysis for a family affected with hemophilia type A due to a large deletion of F8 gene].

Bai N, Mei S, Liu N, Zhao Z, Meng J, Kong X. Bai N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):782-785. doi: 10.3760/cma.j.issn.1003-9406.2016.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984605 Chinese.

7

Factor VIII mutation spectrum in haemophilia A patients in the population of Henan, China.

Bai N, Zhu X, Zhao Z, Bai Y, Wu Q, Liu N, Chen D, Kong X. Bai N, et al. Among authors: bai y. Blood Coagul Fibrinolysis. 2017 Oct;28(7):509-513. doi: 10.1097/MBC.0000000000000628. Blood Coagul Fibrinolysis. 2017. PMID: 28252515

8

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

Qu S, Wang L, Cai A, Cui S, Bai N, Liu N, Kong X. Qu S, et al. Among authors: bai n. J Matern Fetal Neonatal Med. 2019 Jan;32(1):1-10. doi: 10.1080/14767058.2017.1367379. Epub 2017 Oct 16. J Matern Fetal Neonatal Med. 2019. PMID: 29034762 Free article.

9

[Diagnosis of a case with recurrent pregnancy loss resulted from maternal balanced translocation by chromosomal microarray analysis].

Wang L, Bai N, Liu L, Zhang Q, Kong X. Wang L, et al. Among authors: bai n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):443-447. doi: 10.3760/cma.j.issn.1003-9406.2018.03.032. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896752 Chinese.

10

Mutations in the γ-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa.

Shi TW, Bai N, Zhang JA, Lu F, Chen XB, Kong XD, Yu JB. Shi TW, et al. Among authors: bai n. Eur J Dermatol. 2018 Jun 1;28(3):374-376. doi: 10.1684/ejd.2018.3244. Eur J Dermatol. 2018. PMID: 30105992 No abstract available.

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